Product Engineer

ProVerum; Galway; On-site; EUR 65,000 - 90,000; Full time

Benefits offered by this job

Bonus potential

Company pension scheme

Private health insurance

Job summary

ProVerum, a medtech company advancing Benign Prostatic Hyperplasia treatment, seeks a Product Engineer in Galway or Dublin to join the R&D team on-site. You will bridge mechanical design with electronics and software, driving product realization from concept to manufacturing.

You’ll collaborate with cross-functional teams, perform design verification, and contribute to regulatory readiness under ISO 13485 and FDA 21 CFR 820. A hands-on, proactive engineer with SolidWorks experience is ideal.

Qualifications

• Engineering or related technical field is required.
• 3+ years of hands-on medical device experience.
• Experience with electromechanical devices containing software is a plus.

Responsibilities

• Support operations on sustaining the manufacturing line and troubleshoot builds.
• Lead CAPA, NCR, and SCAR investigations through root-cause and closure.
• Design, develop and implement process improvements and fixturing.
• Assist with test/evaluation of new designs and scale-up plans.
• Maintain DHF, QMS procedures and validation documents to regulatory standards.

Skills

Medical devices

Electromechanical design

Cross-functional teamwork

Design verification

Documentation & QA

Education

Engineering degree or related technical field

Tools

SolidWorks

Job description

Location: Galway or Dublin, Ireland | Full-Time, On-site | Reports to: Chief Technical Officer (CTO)

ProVerum is transforming the treatment of Benign Prostatic Hyperplasia (BPH) with minimally invasive technology redefining the standard of care. As we scale, we're looking for a Product Engineer to join our R&D team in Galway or Dublin.

Why ProVerum?

You'll have real ownership, visible impact, and the chance to help shape the future of BPH treatment, working alongside a team that cares deeply about the patients at the end of every decision.

Why you’ll Thrive?

You bridge the worlds of mechanical design with integrated electronics and software to bring products to manufacturing reality. You're comfortable owning complex problems across cross-functional teams from root cause investigations to process scale-up and you take pride in driving compliant, high-quality outcomes in a regulated environment.

You’ll likely have:

• An Engineering or a related technical field
• At least 3 years’ hand on experience in the medical device industry
• Background in electronics and software is a strong advantage, ideally with exposure to electromechanical medical devices containing software
• Experience in product/process validation and design verification/validation
• Knowledge of ISO 13485 and FDA 21 CFR 820 quality and regulatory requirements
• Good mechanical design aptitude with working knowledge of SolidWorks or equivalent CAD package
• Strong written communication skills; confident writing protocols, test reports, and QMS procedures
• A hands-on, proactive attitude with the ability to work effectively in a cross-functional, fast-moving team

In this role you will:

• Support Operations in sustaining the manufacturing line, real-time troubleshooting during builds and leading CAPA, NCR, and SCAR investigations through to root cause and verified closure
• Design, develop and implement process improvements and fixturing; optimise manufacturing processes and production flow in partnership with Operations and Quality
• Support test and evaluation of new and iterative designs; assist with development of product packaging and scale-up plans including staged COGs reduction
• Provide technical support to component and sub-assembly suppliers to ensure quality, reliability, and manufacturing process performance throughout the supply chain
• Maintain DHF, QMS procedures, validation protocols, and reports; ensuring all products, processes, and changes comply with ISO 13485, FDA 21 CFR 820, and applicable regulatory requirements (PMA/510k)

Why Join the ProVerum Team?

Visible impact from day one:

Your work directly supports the devices that reach patients

Build something lasting:

Join at a formative stage and help shape the technical foundations of a company, building SME-level expertise across test methods, materials and manufacturing processes

Collaborative culture:

Work alongside passionate engineers, technicians, and operators who care deeply about product quality and patient outcomes

Competitive package:

Market salary, bonus potential, company pension scheme, private health insurance and more